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BMC Biology
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January 27, 2017
Amyloid-like aggregation of provasopressin in diabetes insipidus and secretory granule sorting
Nicole Beuret, Franziska Hasler, Cristina Prescianotto-Baschong, et al.
European Journal of Endocrinology
|
May 1, 2002
Clinical and molecular analysis of three families with autosomal dominant neurohypophyseal diabetes insipidus associated with a novel and recurrent mutations in the vasopressin-neurophysin II gene
Jonas Rutishauser, Peter Kopp, Mary Beth Gaskill, et al.
Scientific Reports
|
September 22, 2021
Vitamin D oral intermittent treatment (DO IT) study, a randomized clinical trial with individual loading regimen
Jean-Pierre Rothen, Jonas Rutishauser, Philipp N Walter, et al.
BMC Pharmacology & Toxicology
|
July 13, 2020
Oral intermittent vitamin D substitution: influence of pharmaceutical form and dosage frequency on medication adherence: a randomized clinical trial
Jean-Pierre Rothen, Jonas Rutishauser, Philipp N Walter, et al.
Journal of Medical Internet Research
|
May 29, 2024
A Symptom-Checker for Adult Patients Visiting an Interdisciplinary Emergency Care Center and the Safety of Patient Self-Triage: Real-Life Prospective Evaluation
Andreas Meer, Philipp Rahm, Markus Schwendinger, et al.
The Journal of Clinical Endocrinology and Metabolism
|
February 4, 2011
Correlation of plasma copeptin and vasopressin concentrations in hypo-, iso-, and hyperosmolar States
Sandrina Balanescu, Peter Kopp, Mary Beth Gaskill, et al.
European Journal of Endocrinology
|
November 20, 2010
Growth retardation in untreated autosomal dominant familial neurohypophyseal diabetes insipidus caused by one recurring and two novel mutations in the vasopressin-neurophysin II gene
Cécile Brachet, Julia Birk, Catherine Christophe, et al.
The Journal of Biological Chemistry
|
January 13, 2004
Functional characterization of pendrin in a polarized cell system. Evidence for pendrin-mediated apical iodide efflux
Mary P Gillam, Aniket R Sidhaye, Eun Jig Lee, et al.
European Heart Journal
|
October 23, 2020
Acute kidney injury associated with COVID-19: a prognostic factor for pulmonary embolism or co-incidence?
Seyed Soheil Saeedi Saravi, Massimo Barbagallo, Martin F Reiner, et al.
Acta Tropica
|
September 5, 2007
Sleeping glands? - The role of endocrine disorders in sleeping sickness (T.b. gambiense Human African Trypanosomiasis)
Johannes A Blum, Caecilia Schmid, Christoph Hatz, et al.
Page
of 7
Search research articles
Search
Showing results (21-30 of 63) with videos related to
Sort By:
Page
of 7
BMC Biology
|
January 27, 2017
Amyloid-like aggregation of provasopressin in diabetes insipidus and secretory granule sorting
Nicole Beuret, Franziska Hasler, Cristina Prescianotto-Baschong, et al.
European Journal of Endocrinology
|
May 1, 2002
Clinical and molecular analysis of three families with autosomal dominant neurohypophyseal diabetes insipidus associated with a novel and recurrent mutations in the vasopressin-neurophysin II gene
Jonas Rutishauser, Peter Kopp, Mary Beth Gaskill, et al.
Scientific Reports
|
September 22, 2021
Vitamin D oral intermittent treatment (DO IT) study, a randomized clinical trial with individual loading regimen
Jean-Pierre Rothen, Jonas Rutishauser, Philipp N Walter, et al.
BMC Pharmacology & Toxicology
|
July 13, 2020
Oral intermittent vitamin D substitution: influence of pharmaceutical form and dosage frequency on medication adherence: a randomized clinical trial
Jean-Pierre Rothen, Jonas Rutishauser, Philipp N Walter, et al.
Journal of Medical Internet Research
|
May 29, 2024
A Symptom-Checker for Adult Patients Visiting an Interdisciplinary Emergency Care Center and the Safety of Patient Self-Triage: Real-Life Prospective Evaluation
Andreas Meer, Philipp Rahm, Markus Schwendinger, et al.
The Journal of Clinical Endocrinology and Metabolism
|
February 4, 2011
Correlation of plasma copeptin and vasopressin concentrations in hypo-, iso-, and hyperosmolar States
Sandrina Balanescu, Peter Kopp, Mary Beth Gaskill, et al.
European Journal of Endocrinology
|
November 20, 2010
Growth retardation in untreated autosomal dominant familial neurohypophyseal diabetes insipidus caused by one recurring and two novel mutations in the vasopressin-neurophysin II gene
Cécile Brachet, Julia Birk, Catherine Christophe, et al.
The Journal of Biological Chemistry
|
January 13, 2004
Functional characterization of pendrin in a polarized cell system. Evidence for pendrin-mediated apical iodide efflux
Mary P Gillam, Aniket R Sidhaye, Eun Jig Lee, et al.
European Heart Journal
|
October 23, 2020
Acute kidney injury associated with COVID-19: a prognostic factor for pulmonary embolism or co-incidence?
Seyed Soheil Saeedi Saravi, Massimo Barbagallo, Martin F Reiner, et al.
Acta Tropica
|
September 5, 2007
Sleeping glands? - The role of endocrine disorders in sleeping sickness (T.b. gambiense Human African Trypanosomiasis)
Johannes A Blum, Caecilia Schmid, Christoph Hatz, et al.
Page
of 7